Understanding clay mineral transformation is of fundamental importance to grasping phyllosilicate crystal chemistry and unraveling geochemical processes. In this study, hydrothermal experiments were conducted on lizardite and antigorite, to investigate the possibility of the transformation from serpentine to smectite, the effect of precursor minerals' structure on the transformation and the transformation mechanism involved. The reaction products were characterized using XRD, TG, HRTEM, and 27Al MAS NMR. The results show that both lizardite and antigorite can be converted to smectite, but such conversion is much more difficult than that of kaolinite group minerals. The successful transformation is mainly evidenced by the occurrence of the characteristic (001) reflection of smectite at 1.2–1.3 nm in the XRD patterns and smectite layers with a thickness of 1.2–1.3 nm in HRTEM images of hydro-thermal products as well as the dehydroxylation of the newly formed smectite at a higher temperature in comparison to that of the starting minerals. The difficulty for the transformation of serpentine to smectite may be due to the lack of enough available Al in the reaction system, in which the substitution of Al3+ for Si4+ in the neo-formed tetrahedral sheet is critical to control the size matching between the neo-formed tetrahedral sheet and octahedral sheet in starting minerals. Since the neighboring layers in antigorite are linked by the strong Si-O covalent bonds, the transformation only takes place at the edges of an antigorite layer rather than the whole layer, and the neo-formed smectite is non-swelling due to the inheritance of such Si-O covalent bonds. The conversion of lizardite to smectite is more feasible than that of antigorite, accompanied by exfoliation. This leads to a prominent decrease of the particle size in the hydrothermal products and the number of phyllosilicate layers contained therein. Two dominant pathways were observed for the transformation of lizardite and antigorite into smectite, i.e., conversion of one serpentine layer to one smectite layer via attachment of Si-O tetrahedra onto the octahedral sheet surface of the starting minerals and two adjacent serpentine layers merging into one smectite layer. In the case of the latter, dissolution of octahedra and inversion of tetrahedral sheets took place during the transformation. Besides these two dominant pathways, precipitation and epitaxial growth of smectite were also observed in the cases of lizardite and antigorite, respectively. The present study suggests that solid-state transformation is the main mechanism for conversion of serpentine minerals to smectite, similar to the transformation of kaolinite group minerals to beidellite.
Clay minerals are ubiquitous on the Earth's surface that can be transformed into other phyllosilicates in various geological and geochemical processes (e.g., weathering, diagenesis, and meta-morphism) (Wildman et al. 1968; Dunoyer de Segonzac 1970; Hower et al. 1976; Lanson et al. 1996; Stripp et al. 2006). Transformation mechanisms and resulting products are controlled by geochemical environments in which a transformation takes place. Accordingly, chemical changes and mineralogical transformations can provide important constrains for the geochemical conditions that cause these processes. And, in turn, these transformations can exert influences on the cycling of elements in the related environments, due to the high surface-to-volume ratio and surface reactivity of clay minerals (Cuadros 2012).
So far, mostly reported are the transformations among 2:1 type clay minerals (e.g., illitization of smectite, glauconitization of smectite) (Weaver 1958; Boles and Franks 1979; Odin 1988; Lindgreen et al. 2000) and from 2:1 type to 1:1 type (e.g., kaolinization of smectite) (Altschuler et al. 1963; Righi et al. 1999; Ryan and Huertas 2013). Chloritization of 1:1 type clay minerals (e.g., serpentine, berthierine) (Banfield and Bailey 1996; Xu and Veblen 1996; Ryan and Reynolds 1997), a conversion of 1:1 type to 2:1 type, mainly takes place in the subsurface of geological systems (Beaufort et al. 2015). Based on the investigations of natural and synthetic samples, two mechanisms have been proposed for clay transformations: (1) conversion in solid state by atom rearrangement with the interlayer as the main route for atom diffusion in and out of the structure; (2) dissolution of the original mineral and recrystallization of the new structure phase (Pollard 1971; Nadeau et al. 1985; Dudek et al. 2006; He et al. 2017). The reported studies suggest that the solid-state transformation mechanism prevails in weathering environments (Mackumbi and Herbillon 1972; Banfield and Murakami 1998; Wilson 2004), while in diagenetic and hydro-thermal environments, the occurrence of either solid-state or dissolution-recrystallization transformation appears to be largely controlled by fluid-to-rock ratio (Altaner and Ylagan 1997).
In comparison to the transformation pathways among 2:1 type clay minerals and from 2:1 type to 1:1 type, the conversion of 1:1 type clay minerals to 2:1 type ones is less commonly observed on the Earth's surface. As reported in literature (Coombe et al. 1956; Ducloux et al. 1976; Istok and Harward 1982; Graham et al. 1990; Bonifacio et al. 1997; Lee et al. 2003), 2:1 type clay minerals are mainly formed in the procedures of weathering and pedogenesis, in which 1:1 type clay minerals were dissolved and provided the elemental sources for recrystallization of 2:1 type ones, i.e., a dissolution-recrystallization mechanism is involved in the transformations. Recently, our hydrothermal experiments show that both kaolinite and halloysite (i.e., 1:1 type clay minerals) can be converted to beidelite (i.e., 2:1 type clay minerals) via a solid-state mechanism (He et al. 2017). In this procedure, attachment of a newly formed Si-O tetrahedral sheet to the 1:1 layer of precursor mineral is a critical step for successful transformation. Simultaneously, the substitution of Al3+ for Si4+ in the neo-formed tetrahedral sheets can greatly improve the size matching between the octahedral sheet of the precursor mineral and the neo-formed tetrahedral sheet. However, a few new insights and further clarifications are needed, including: (1) whether other 1:1 type clay minerals (e.g., serpentine), besides kaolinite and halloysite, can be converted to smectite under hydrothermal condition? (2) What is the effect of the precursor phase structure on the transformation? (3) Whether isomorphous substitutions in the neo-formed tetrahedral sheets (e.g., Al3+ for Si4+) is essential for the conversion of serpentine to 2:1 type clay minerals? (The Al content in serpentine minerals is much lower than that in kaolinite group minerals.) Hence, this paper, as a companion study of our recent work on the transformation of kaolinite and halloysite to beidellite (He et al. 2017), reports our latest investigations on the transformation of serpentines (e.g., lizardite and antigorite) into smectite under identical hydrothermal condition.
Materials and methods
Two kinds of serpentine minerals with different structures, lizardite and anti-gorite, were used in the transformation experiments. The lizardite sample (L) was collected from Taitung County, Taiwan Province, China, and the geological details were summarized by Chang et al. (2000). The antigorite sample (A) was collected from the serpentinized dolomitic marble, which belongs to Proterozoic carbonate strata (Xiuyan County, Liaoning Province, China). Their chemical compositions are presented in Table 1, determined by using X-ray fluorescence spectroscopy (XRF) (He et al. 2014).
Lizardite has a flat crystal structure with the correct geometry of interlayer H-bonds, which is favored by the coupled substitution of Al3+ or Fe3+ for Mg2+ in octahedral sheets and Si4+ in tetrahedral sheets (Evans et al. 2013). Antigorite displays curved, wavy layers similar to Roman tiles on a roof. The octahedral sheet is continuous and wavy, whereas the tetrahedral sheet undergoes periodic reversals along the a axis so that it connects to the concave half-waves of adjacent octahedral sheets (Otten 1993; Grobéty 2003; Capitani and Mellini 2004; Evans et al. 2013). The reversals allow serpentine layers to be bound through strong covalent Si–O bonds (Evans et al. 2013). The large superstructure of antigorite along the  direction is a result of this repeating wave structure (Zussman 1954; Kunze 1956, 1958, 1961; Uehara 1988). In this study, the supercell repeat-unit in antigorite is approximately 3.1 nm, which is determined by the selected-area electron diffraction (SAED) patterns (see HRTEM observation and EDS analysis) (Whittaker and Zussman 1956; Zussman et al. 1957; Kunze 1961; Uehara and Shirozu 1985; Uehara 1988; Palacios-Lidon et al. 2010).
Sodium metasilicate (Na2SiO3·9H2O) of analytical grade was used as the Si source for the transformation experiments.
The hydrothermal experiments were conducted in a stainless steel autoclave at 300°C under an autogenous water pressure. The Mg/Si ratios in the starting mixture of sodium metasilicate and serpentine were fixed at 3:4, close to that of saponite. The experiment procedure was as follows: 24 g of sodium metasilicate was dissolved into 100 mL deionized water with continuous stirring. The pH of the solution was adjusted to 8 by hydrochloric acid under vigorous stirring. Then, the obtained sol-gel was transferred into a stainless steel autoclave and mixed with 3.5 g of serpentine. The mixture was hydrothermally treated in the autoclave at 300°C under an autogenous water pressure for one to two weeks. The obtained products were washed 6 times using deionized water to remove electrolytes, and then dried at 80°C for 24 h and ground before characterization. The products were marked as X-xw, in which X = L or A, standing for lizardite or antigorite, respectively, and xw stands for the duration of the treatment time, i.e., 1w = 1 week and 2w = 2 weeks. The experimental conditions adopted in this study are summarized in Table 2.
|t (w)a||Sample||T (°C)||P (MPa)b||XRDc||TEMd||%Se|
|Products from lizardite|
|Products from antigorite|
|t (w)a||Sample||T (°C)||P (MPa)b||XRDc||TEMd||%Se|
|Products from lizardite|
|Products from antigorite|
a t stands for the duration of the treatment time and w is short for week, i.e., 1w = 1 week and 2w = 2 weeks.
bP is the autogenous water pressure at 300°C.
c Only the basal spacings of neo-formed smectite are listed for the hydrothermal products.
d The values are determined based on selected area electron diffractions.
e The ratio of the newly formed smectite (S) in the hydrothermal products, determined by the powder XRD patterns.
X-ray diffraction (XRD). XRD patterns were collected on a Bruker D8 Advance diffractometer with Ni-filtered CuKα radiation (λ = 0.154 nm, 40 kV and 40 mA) at a scanning rate of 1° (2θ) min–1 between 3 and 30° (2θ). The powder XRD patterns were used for the determination of mineral contents in the hydrothermal products, where pure Si was selected as the internal standard. The methods for sample preparation and the mineral content analysis were described by Brindley (1980b). The oriented samples were prepared by adding 15 mg solid products into 1 mL deionized water, followed by ultrasonic dispersion for 2 min. Then, the suspension was added onto a glass slide dropwise and dried at ambient temperature. Glycolated samples were prepared by treating the oriented samples in a glass desiccator with ethylene glycol at ambient temperature for 24 h.
Thermogravimetric analysis (TG). TG analyses were performed on a Netzsch STA 409PC instrument. Approximately 15 mg ground sample was heated in a corundum crucible from 30 to 1000°C at a heating rate of 10°C/min under a pure N2 atmosphere (60 cm3/min). The differential thermogravimetric (DTG) curve was derived from the TG curve.
High-resolution transmission electron microscopy (HRTEM). To investigate the silicate layers of entire crystals or particles in the direction parallel to the c axis, sample are oriented embedded in epoxy resin. Then, ultrathin sections (~75 nm) were ultramicrotomed with a diamond knife using a Lecia EM UC7 and mounted on holey carbon-coated TEM copper grids. HRTEM images, X-ray energy-dispersive spectroscopy (EDS), and selected-area electron diffraction (SAED) analyses were carried out using a FEI Talos F200S high-resolution transmission electron microscope equipped with Super-X X-ray spectroscopy, and operated at 200 kV.
Magic-angle-spinning nuclear magnetic resonance spectroscopy (MAS NMR).27Al MAS NMR spectra were obtained on Bruker AVANCE III 600 spectrometer at resonance frequency of 156.4 MHz. A 4 mm HX double-resonance MAS probe was used to measure 27Al MAS NMR at a sample spinning rate of 14 kHz. The spectra were recorded by a small-flip angle technique with a pulse length of 0.5 μs (<π/12) and a 1 s recycle delay. The chemical shift of 27Al was referenced to 1 M aqueous Al(NO3)3.
XRD patterns of both lizardite and antigorite display characteristic basal spacings at 0.72 nm (Mellini 1982; Uehara and Shirozu 1985) without any reflections from impurity minerals (Fig. 1), indicating that the starting minerals are of high purity. In the case of lizardite, the intensity of (001) reflection dramatically decreases after hydrothermal treatment, which is accompanied by the occurrence of three new reflections at 0.33, 0.42, and 1.27 nm, respectively (Fig. 1a). The intense reflections at 0.33 and 0.42 nm correspond well to (101) and (100) planes of quartz, which are formed by the polymerization of metasilicate (Wooster and Wooster 1946). Upon ethylene glycolation, the reflection at approximately 1.27 nm shifts to 1.70 nm, displaying a swelling property of the corresponding mineral. This suggests the newly formed mineral should be smectite (Mosser-Ruck et al. 2005; He et al. 2017). As one of the starting materials is Na2SiO3·9H2O, the resultant smectite may have Na+ as its interlayer cation, consistent with the d001 of 1.27 nm (Suquet et al. 1975; Ferrage et al. 2010).
It is noteworthy that the characteristic reflections of the neo-formed smectite is very weak and broad, implying poor crystallinity as well as low layer-stacking order (He et al. 2014). Meanwhile, as indicated by XRD patterns (Fig. 1), the reflection intensity of quartz increases with the extension of hydrothermal reaction duration from one week (L-1w) to two weeks (L-2w). Since the stoichiometric ratios of Mg/Si in the starting materials are 3:4, close to that of saponite, the formation of quartz suggests that only part of the added metasilicate involves in the transformation and the conversion of lizardite to smectite (i.e., saponite in this study) is more difficult than halloysite and kaolinite (He et al. 2017).
The transformation of antigorite seems to be different from that of lizardite, indicated by XRD patterns (Figs. 1d–1f). After hydrothermal treatment, the reflections of antigorite are still prominent with a slight decrease of the reflection intensity [e.g., the (001) reflection at 0.72 nm]. Simultaneously, the characteristic reflections of newly formed quartz and smectite are observed at 0.33 and 1.24 nm, respectively (Fig. 1d). It is noteworthy that an intense (001) reflection of neo-formed smectite at 1.24 nm was recorded in the oriented XRD pattern of the two weeks' hydrothermal product (A-2w-O). More importantly, this basal spacing does not have any change upon ethylene glycolation (Fig. 1f), implying that the microstructure of hydrothermal products is different from the ones transformed from lizardite in this study and those from kaolinite group minerals (Ryu et al. 2006; He et al. 2017).
The TG and DTG curves of samples are presented in Figure 2. A prominent mass loss of lizardite, corresponding to dehydroxylation, occurs at approximately 608°C, while the mass loss of adsorbed water was recorded at around 100°C (Fig. 2a). The dehydroxylation temperature of lizardite in this study is obviously lower than that of serpentine minerals (i.e., lizardite, antigorite, and chrysotile) reported by Viti (2010). After hydrothermal treatment, the mass loss of dehydroxylation dramatically decreases and a new mass loss occurs at approximately 750°C (Figs. 2b and 2c). The significant decrease of the dehydroxylation mass loss is attributed to the consumption of inner-surface hydroxyls in starting minerals during the transformation of 1:1 type clay minerals into 2:1 type ones (He et al. 2017). Theoretically, about two-thirds of inner-surface hydroxyls in 1:1 type precursor minerals will be consumed during the transformation, through the condensation between inner-surface hydroxyls and hydrolyzed metasilicate (He et al. 2017).
The TG and DTG curves of antigorite and its hydrothermal products display prominent differences in comparison to those of lizardite and its hydrothermal products (Figs. 2d–2f). The TG curve of antigorite only shows one main mass loss around 740°C, corresponding to dehydroxylation, and no obvious mass loss of adsorbed water was observed at approximately 100°C (Fig. 2e). Dehydroxylation temperature of antigorite is different from those reported in literature (Viti 2010), in which the main mass loss of dehydroxylation occurs at 713–720°C, coupled with a mass loss at higher temperature (e.g., 743–760°C) and a shoulder at lower temperature (e.g., 636–645°C). For the hydrothermally treated products, the starting and end temperatures of the dominant mass loss, corresponding to the dehydroxylation of antigorite, are almost identical to those of the precursor mineral while the center of corresponding DTG peak shifts to 720°C (Figs. 2e and 2f). Simultaneously, a minor mass loss occurs at approximately 830°C (Figs. 2e and 2f), attributed to the dehydroxylation of the newly formed smectite. The thermal analysis results suggest that most of the antigorite precursor remains unchanged with a minor part converted to smectite, in agreement with the XRD results (Fig. 1d).
HRTEM observation and EDS analysis
HRTEM images of both lizardite and antigorite before and after hydrothermal treatments clearly display prominent morphological changes and structural evolution of clay mineral layers (Figs. 3–6). Generally, both newly formed smectite layers with a thickness of 1.2–1.3 nm (Schumann et al. 2013) and the serpentine layers of the starting minerals with a thickness of approximately 0.7 nm are observed in all hydrothermal products. X-ray EDS analyses reveal that the Si/Mg ratios of the newly formed smectite layers are almost identical with the reported values in smectite (Fig. 7) (Bergaya and Lagaly 2013). These results demonstrate that both lizardite and antigorite can be successfully transformed into smectite, consistent with the XRD results.
In the case of lizardite, smectite layers occur not only at the edge of the lizardite layers, but also within lizardite domains after hydrothermal treatment (Fig. 3). The starting mineral displays regular stacking layers with a thickness of 0.7 nm (Fig. 3a). However, after hydrothermal treatment, distorted phyllosilicate layers are extensively observed within lizardite domains, where the transformation of lizardite into smectite takes place (indicated by the white arrows in Fig. 3b). The layer-stacking order of lizardite was destroyed by these distortions, and large lizardite particles were split into several smaller ones. Meanwhile, the particle size in Sample L-2w (Fig. 3c) is smaller than that in Sample L-1w (Fig. 3b), implying that the particle size and the number of phyllosilicate layers contained therein deceases with an extension of hydrothermal treatment time. This may lead to the weak (001) reflections of the hydrothermal products from lizardite (Figs. 1a–1c) (Brindley 1980a).
Two different pathways are observed in the transformation of lizardite into smectite. As shown by the HRTEM images of L-1w (Figs. 3d and 3e, enlarged areas of the outlined areas in Fig. 3b), the lizardite layers were directly converted to the same number of smectite layers at the left part, while two smectite layers were formed from three lizardite layers at the right part. More interestingly, the HRTEM images (the right part in Figs. 3d and 3e) clearly show that one of the three lizardite layers was converted to one smectite layer while the other two lizardite layers merged into one smectite layer. Similar transformation pathways are also observed in Sample L-2w, in which four lizardite layers were transformed into three smectite layers (Fig. 3f, enlarged area of the outlined area in Fig. 3c). These observations suggest that the smectite layers can be formed through different pathways from lizardite layers. Besides the dominant particles with coexistence of lizardite and smectite layers, a small amount of pure smectite particles without any lizardite layers are also observed in the hydrothermal products (Fig. 4). Most of these particles consist of only 3–20 smectite layers, and the size is significantly smaller than that of the particles with a coexistence of lizardite and smectite layers.
For the hydrothermal products from antigorite, neo-formed smectite layers only occur at the edges of antigorite particles (i.e., the neo-formed smectite layers are only formed at the edges of antigorite layers) (Figs. 5 and 6). Simultaneously, no significant decrease of particle size and distortion of antigorite layers is observed. These morphological characteristics are very different from the products from lizardite and can well explain the intense (001) reflection of antigorite in the hydrothermal products (Figs. 1d–1f). The length of the newly formed smectite layers at the edges of antigorite particles is approximately 5 nm in Sample A-1w, with poor crystallinity as well as low layer-stacking order (Fig. 5b), resulting in the weak basal reflections of smectite in the XRD patterns (Figs. 1d and 1e). With an extension of hydrothermal treatment time, the length of the smectite layers becomes slightly longer (5–10 nm) and the layer-stacking order is increased. A small amount of smectite layers with several tens of nanometers in length can also be observed (Fig. 6). Since one end of the newly formed smectite layers, connecting with antigorite layers, is linked by the strong covalent Si–O bonds and they are very short in length as shown by HRTEM images (Figs. 5–6), the resulting smectite may not show swelling property. This is evidenced by the XRD measurements in which the basal reflection of smectite did not shift to 1.70 nm upon ethylene glycolation (Fig. 1f). Due to the very low Al content in the starting antigorite (Table 1), the newly formed smectite might be of low charge density.
Similar to the case of lizardite, both the merging of two antigorite layers into one smectite layer and the conversion of one antigorite layer to one smectite layer are observed. The former will lead to the number of neo-formed smectite layers obviously less than that of the neighboring antigorite layers (Fig. 5c). It is noteworthy that the length of a half supercell repeat-unit in antigorite is approximately 1.6 nm (i.e., the length of a supercell periodicity is ~3.1 nm), which is shorter than the length of the neo-formed smectite layers. This implies that the epitaxial growth of smectite layers might be also involved in the transformation procedure. These observations suggest that the structural difference between lizardite and antigorite has significant effects on the transformation and the mechanism involved.
EDS analyses supply supporting evidences for the successful transformation of lizardite and antigorite into smectite. The Si/Mg ratios of the neo-formed smectite layers are located in the range of 1.1–1.4 (Fig. 7), which is almost identical with the values of reported smectite. The Al/Mg ratios of the newly formed smectite are slightly higher than that of the corresponding lizardite and antigorite. This implies that the substitution of Al3+ for Si4+ may occur in the transformation of serpentine minerals into smectite, which is identified by 27Al MAS NMR spectra.
27Al MAS NMR spectra
27Al MAS NMR spectrum of lizardite (Fig. 8a) displays a very weak and broad signal centered at 7.7 ppm, corresponding to sixfold-coordinated Al [Al(VI)] in octahedral sheets (Woessner 1989; Bentabol et al. 2010). In 27Al MAS NMR spectra of hydrothermal products from lizardite, the signal at 7.7 ppm almost disappears and a new signal occurs at approximately 68 ppm (Fig. 8a), corresponding to the fourfold-coordinated Al [Al(IV)] in the Si-O tetrahedral sheets via the substitution of Al3+ for Si4+ (Woessner 1989; Bentabol et al. 2010). This implies the migration of Al3+ from octahedral sheets to tetrahedral ones during the transformation under hydrothermal condition (He et al. 2017).
The 27Al MAS NMR spectrum of antigorite contains two signals at approximately 10 and 69 ppm (Fig. 8b), attributed to Al(VI) in octahedral sheets and Al(IV) in tetrahedral ones, respectively. After hydrothermal treatment, the Al(VI) signal at ca. 10 ppm decreases while that of Al(IV) signal obviously increases. Simultaneously, a new signal appears at approximately 60 ppm (Fig. 8b), which is assigned to Al in the three-dimensional silica framework (Breen et al. 1995). The intensity of this signal obviously increases with an extension of hydrothermal treatment time (Fig. 8b). As indicated by XRD patterns (Fig. 1), quartz formed during the transformation due to the polymerization of metasilicate. Thus, the signal at approximately 60 ppm should be attributed to the incorporation of Al into the newly formed quartz (He et al. 2017). These Al atoms are released into the solution due to the dissolution of octahedral sheets in serpentine minerals during the transformation.
Transformation from serpentine to smectite
Smectites are 2:1 type clay minerals with isomorphic substitutions in tetrahedral and/or octahedral sheets. The substitutions between cations with different valences result in the permanent negative layer charge, which is compensated by exchangeable cations in the interlayer spaces. Subsequently, the basal spacing (d001) of smectite is controlled by the nature of interlayer cations and their hydration state. For instance, Na-smectite with one-water layer in the interlayer space has a basal spacing of 1.2–1.3 nm (Ferrage et al. 2005). The occurrence of the reflections at 1.2–1.3 nm in the XRD patterns of the hydrothermal products (Fig. 1) is indicative of the formation of smectite (Sato et al. 1992; Ferrage et al. 2005). As Na2SiO3·9H2O was used as one of the starting materials, the resultant smectite may have Na+ as its interlayer cation. Meanwhile, TEM observations also provide convincible evidences for the successful transformation from serpentine to smectite. After hydrothermal treatment of lizardite and antigorite, the smectite layers with a thickness of approximately 1.3 nm can be extensively observed in the TEM images (Figs. 3–6) (Murakami et al. 1999; Kim et al. 2004; Bisio et al. 2008; He et al. 2017). And the Si/Mg ratios of these layers, determined by EDS analyses, are almost identical with that of smectite (Fig. 7).
Note that the changes of XRD patterns for lizardite and antigorite before and after hydrothermal treatment are dramatically different. For antigorite, the XRD patterns of hydrothermal products display prominent reflections of antigorite precursor, suggesting that most parts of antigorite remain unchanged. This is also supported by the HRTEM images in which the newly formed smectite is only observed at the edge of the antigorite particles rather than within them. However, in the case of lizardite, despite the weak reflection of smectite, the characteristic (001) reflection at 0.72 nm dramatically decreased after hydrothermal treatment. HRTEM observations indicate that the conversion of lizardite to smectite can occur in different domains within lizardite particles, accompanied by layer distortion and exfoliation. This may result in the dramatic decrease of characteristic reflection of lizardite and the occurrence of weak reflections of smectite (Lan and Pinnavaia 1994; Watkins and McCarthy 1995; Dennis et al. 2001). The occurrence of intense reflections of quartz [e.g., (101) and (100) reflections] in the XRD patterns of hydrothermal products and the increase of their intensity with an extension of reaction time strongly suggests that the added metasilicate did not completely react with serpentine minerals, and polymerization of metasilicate led to the formation of quartz.
Compared to the transformation of kaolinite and halloysite into smectite (He et al. 2017), the transformation of serpentine (e.g., lizardite and antigorite) into smectite is much more difficult. In our recent studies (He et al. 2014, 2017), the substitution of Al3+ for Si4+ in the tetrahedral sheets has been proved to be critical for improving the size matching between octahedral and tetrahedral sheets of smectite. EDS analyses of the hydrothermal products show that the Al/Mg ratios of the newly formed smectite are slightly higher than that of the corresponding serpentine minerals (Fig. 7). This suggests that Al atoms are incorporated into the neo-formed smectite during the transformation, which are provided by the dissolution of the octahedral sheets of the starting serpentine. Our 27Al MAS NMR spectra further demonstrate that these Al atoms enter into the Si-O tetrahedral sheets via the substitution of Al3+ for Si4+. Thus, the difficulty of the transformation from serpentine to smectite may be due to the low Al content in the starting serpentine minerals (Table 1), which is the available Al source for the substitution of Al3+ for Si4+. Our calculation, based on the powder XRD patterns, shows that the ratios of the newly formed smectite in the hydrothermal products from antigorite (A-2w) and lizardite (L-2w) are 28.3 and 57.3% (Table 2), respectively. Such significant difference between the transformation ratios from antigorite and lizardite may be mainly controlled by their structure and the transformation mechanism involved as well as the low Al content in precursor minerals.
The structural unit of serpentine has a polar layer with a thickness of 0.72 nm, which is composed of one tetrahedral sheet and one octahedral sheet (Wicks and Whittaker 1975; Mellini 1982; Grobéty 2003; Palacios-Lidon et al. 2010; Evans et al. 2013). Lizardite and antigorite have similar theoretical formula of Mg3Si2O5(OH)4 but with different extents and types of isomorphous substitution (e.g., lizardite is rich in Al and Fe, and antigorite is rich in Si) (Uehara and Shirozu 1985; O'Hanley and Dyar 1993). The linking ways of neighboring layers for serpentine minerals are very different from each other. The adjacent layers in lizardite are linked via hydrogen bonds. However, in antigorite, the octahedral sheet is continuous and wavy, whereas the tetrahedral sheet undergoes periodic reversals. Thus, antigorite layers are bound through strong covalent Si-O bonds connecting the reversals (Evans et al. 2013). For smectite, its unit layer consists of an octahedral sheet sandwiched between two opposing tetrahedral sheets (Kloprogge et al. 1999; Bisio et al. 2008). Due to isomorphous substitutions (e.g., Al3+ by Mg2+, or Mg2+ by Li+, in the octahedral sheet; and Si4+ by Al3+ in the tetrahedral sheet), the layers are negatively charged, which is balanced by exchangeable interlayer cation (Brigatti et al. 2013). According to the essential structural difference between serpentine and smectite, one Si-O tetrahedral sheet must be attached onto the octahedral sheet of serpentine if the transformation of serpentine to smectite takes place via solid-state mechanism.
As indicated by the HRTEM images (Fig. 3), two dominant transformation pathways take place in the conversion of lizardite to smectite. One is the conversion of lizardite layers to the same number of smectite layers (Figs. 3d–3f) through the reaction of TO (lizardite layer) + T → TOT (smectite layer) (Fig. 9a). The extra tetrahedral sheets (T) are formed through attachment Si-O tetrahedra (i.e., hydrolyzed metasilicate in reaction solution) onto the octahedral sheets of the lizardite layers, which is followed by condensation between inner-surface hydroxyls and hydrolyzed metasilicate (He et al. 2017). This suggests a solid-state mechanism involved in the transformation (Amouric and Olives 1998; He et al. 2017). Thus, the thickness of the neo-formed layers increases to 1.3 nm from 0.7 nm in lizardite, in which the expansion of the newly formed smectite layer results in squeezing the interlayer space between the smectite layer and its adjacent lizardite layer (Figs. 3d and 3e). This will lead to distortion and exfoliation of phyllosilicate layers in the hydrothermal products and significant decrease of particles size and layer number contained therein (Fig. 9a), consistent with the weak (001) reflections of the hydrothermal products (Fig. 1a). Such transformation procedure is similar to that from kaolinite to beidellite as our previous report (He et al. 2017).
The other pathway is merging of two lizardite layers into one smectite layer through a reaction of 2TO → TOT + Mg2+/Al3+, which is accompanied with dissolution of octahedral sheets and inversion of one tetrahedral sheet in one lizardite layer (Fig. 9a). Such conversion via partial dissolution of the initial serpentine structure (i.e., octahedral sheet) with recombination of Si-O sheet and serpentine layer to form smectite layers can also be regarded as solid-state transformation (Altaner and Ylagan 1997; Amouric and Olives 1998; Banfield and Murakami 1998; Cuadros and Altaner 1998; Lindgreen et al. 2000; Dudek et al. 2006; Cuardos 2012). As shown by HRTEM images (Fig. 3c), 15 lizardite layers (TO) are observed at the central area of Sampler L-2w (left red rectangle in Fig. 3c), while only 8 smectite layers (TOT) occur at the edge of this particle (right red rectangle in Fig. 3c). This strongly suggests that dissolution of Mg-octahedral sheets took place during the transformation. However, our measurements show that the concentration of Mg in the supernatant solution is lower than 1 ppm. This seems to be contradictory with the proposal about the dissolution of Mg-octahedral sheets. Our HRTEM observation shows that a small amount of pure smectite particles, without any lizardite layers, occurs in the hydrothermal products (Fig. 4). As no additional Mg source was added into the reaction system, in which lizardite is the only phase containing Mg. Hence, these pure smectite particles should be formed by the reaction between the dissolved Mg and metasilicate, resulting in a very low Mg concentration in the solution. This reflects that a dissolution-reprecipatation mechanism is also involved in the transformation, but not as dominant as solid-state transformation.
In comparison to lizardite, the transformation of antigorite into smectite is much more difficult. Our calculation, based on the powder XRD patterns, shows that only 28.3% of anti-gorite was successfully converted to smectite. The calculated result is well coincident with the HRTEM observations of the hydrothermal products, in which the newly formed smectite layers were only formed along the edges of the starting anti-gorite particles and no smectite layers were observed within the antigorite domains (Fig. 5b). This is very different from the transformation of lizardite as discussed above. The occurrence of such transformation is due to the unique structure of antigorite. For the supercells in the inner part of antigorite layer, both the ends are fixed by the strong Si-O covalent bonds between the two adjacent layers (Evans et al. 2013), hindering the transformation from antigorite to smectite. However, for the supercell at the edge of a certain layer, the end toward inner side is fixed by the covalent Si-O bond whereas the other end toward outside does not have such fixation, similar to the lizardite layer to some extent. Accordingly, both the two transformation pathways, conversion of one antigorite layer to one smectite layer and two adjacent antigorite layers merging into one smectite layer, occur at the edge of antigorite particles (Figs. 5c and 9b), corresponding to a solid-state mechanism (Banfield and Bailey 1996; Xu and Veblen 1996; Amouric and Olives 1998; He et al. 2017). As indicated by the HRTEM images (Fig. 5c), newly formed smectite layers are well connected with the antigorite layers, and the length of the neo-formed smectite layers is longer (most located at the range of 5–10 nm, Figs. 5 and 6) than that of a half the supercell repeat-unit in antigorite (approximately 1.6 nm). This reflects that epitaxial growth of smectite layers is also involved in the transformation, which could be regarded as a dissolution-reprecipatation procedure. As antigorite is the only phase containing Mg and no additional Mg source was added in this reaction system, the released Mg, due to the dissolution of octahedral sheet, is the main Mg source for epitaxial growth of smectite layers (Starcher et al. 2017).
To exclude the potential effects of the starting mineral dissolution on their transformation, dissolution experiments were conducted under the identical conditions but without adding any sodium metasilicate. No reflections at approximately 1.3 nm, corresponding to the basal spacing of smectite, were recorded in the XRD patterns of the hydrothermal products (not show). This is consistent with their HRTEM images (not show) in which no smectite layers and distortion of serpentine layers were observed. Meanwhile, our measurements showed that the Mg concentration in the supernatant solution is as low as 2–3 ppm. These investigations suggest that no significant dissolution of the starting serpentine minerals took place under the identical P-T condition (without adding Si source). In other words, an existence of additional Si source is essential for the transformation of serpentine into smectite. This is in agreement with the insights deduced from the conversion of halloysite and kaolinite to beidellite (He et al. 2017).
Our present study demonstrates that 1:1 type serpentine minerals (i.e., lizardite and antigorite) can be transformed into 2:1 type smectite under hydrothermal condition. In this procedure, one serpentine layer can be converted to one smectite layer via attachment of Si-O tetrahedra onto the octahedral sheet surface of the starting minerals, and two adjacent serpentine layers can be merged into one smectite layer (Fig. 9). In the latter case, dissolution of Mg-octahedral sheets and inversion of tetrahedral sheets take place. Both the two pathways suggest that the solid-state mechanism is involved in the transformation of serpentine minerals into smectite (Banfield and Bailey 1996; Xu and Veblen 1996; Amouric and Olives 1998; He et al. 2017). Due to the dissolution of Mg-octahedral sheets, free Mg cations are released into the reaction system and they can react with metasilicate to form smectite. Certainly, a small amount of Al cations are simultaneously released in this procedure and most of them are incorporated into the newly formed Si-O tetrahedral sheets of smectite, as indicated by 27Al MAS NMR spectra. Such substitution of Al3+ for Si4+, which can improve the size matching between octahedral and tetrahedral sheets of smectite, has important effect on a successful transformation and conversion rate from serpentine to smectite. However, in comparison to the transformation of kaolinite group minerals to beidelite under identical experimental conditions, the transformation of serpentine minerals is more complex. Besides the solid-state transformation ways, epitaxial growth of smectite occurred in the conversion of antigorite while precipitation happened in the case of lizardite. This suggests that the microstructure of the starting minerals have important effects on their transformation procedures and crystallochemical characteristics of the resulting minerals. This insight would be helpful for better understanding phyllosilicate crystal chemistry. For example, due to the adjacent antigorite layers linked by the strong Si-O covalent bonds, the epitaxial growth of smectite was observed in the transformation. Similarly, the neighboring layers in mica group minerals are linked via strong electrostatic force, and they always display large particle size. This implies that a strong physicochemical interaction (as well as similarity in chemical compositions) between the adjacent layers in phyllosilicates (Charlet and Manceau 1994; Ji et al. 2013; Yang et al. 2015; Starcher et al. 2017) is critical for epitaxial growth. Maybe, this can well explain the interesting phenomenon that mica group minerals always display large crystal size, whereas the size of smectite group minerals are less than several micrometers.
On the other hand, serpentine minerals are an important component of the oceanic crust, and they play a chief role in lithosphere dynamics (Viti 2010). Our present experimental study demonstrates that the transformation of serpentine into smectite is feasible, especially for lizardite, under hydrothermal environment with the presence of SiO2, but without any evidence for the formation of talc. However, voluminous literature reported that serpentine could be converted to talc in SiO2-rich fluid systems without occurrence of smectite. Due to chemical and structural variations, talc and smectite have significant differences in water content, cation mobility, and physicochemical properties. Thus, they can exert great influences on rock volume, rock rheology, and rock permeability, with subsequent effects on subduction zones, fault dynamics, and seismic behavior (Moore and Saffer 2001; Peacock 2001; Moore and Rymer 2007; Lockner et al. 2011). Our present study implies the possibility for the conversion of serpentine to smectite in nature. Hence, detailed mineralogical identification of hydrothermal products of serpentine in various natural systems, as well as comprehensive investigations on the geochemical conditions for occurrence of talc and/or smectite transformed from precursor serpentine, are needed in further study.
This is contribution No. IS-2473 from GIGCAS. This work was financially supported by National Natural Science Foundation of China (Grant Nos. 41530313), CAS Key Research Program of Frontier Sciences (Grant No. QYZDJ-SSWDQC023), the CAS/SAFEA International Partnership Program for Creative Research Teams (Grant No. 20140491534) and Natural Science Foundation of Guangdong Province, China (Grant No. S201303001424). The authors thank Warren Huff for handling this paper, and Alain Decarreau and Huifang Xu for reviewing the manuscript and providing constructive comments.